Will leave this here and go for my tea, as I'm in a horrendous mood and might say something I regret.
Mod note: This post has been copied to the thread about the article here:
Health Sense article: Why deny patients with chronic fatigue syndrome treatments that can help?, 2022, by Peter White
This post and a couple of replies copied from the Paul Garner thread.
Will leave this here and go for my tea, as I'm in a horrendous mood and might say something I regret.
Managed to get the updated BACME name, but still got it wrong!
Pete Gladwell is one of the more active BACME members, and has been part of the dysregulation stuff.
I've been following this up with Sonya, and I am getting the impression that there has been an active decision not to publish the meeting minutes, and that this has come from Carol Monaghan.
I do not think we're going to see the historical minutes or future minutes readily and timely added to...
I would not be surprised by this. I have all sorts of issue with my vision, and particularly visual processing. There hasn't been much work on vision/eyes and M.E—except a few studies at the University of Leicester.
https://onedrive.live.com/?authkey=%21AGlC5G370Oiz4%2D8&id=BF7ACC05412B947D%21688083&cid=BF7ACC05412B947D
Historical minutes for 2020–2021 meetings, uploaded by a patient (more here...
It suggests shift in gear, and also ambition, which is much needed. We're not going to get anywhere with £100k here and £100k there. I hope this pays dividends.
I agree. You'd usually see this post in a university department where there might be numerous grant-winning staff who need a bit of help and overall vision/strategy. There are barely any funds to supervise! Mainly DecodeME, but that should surely be being done by someone at Edinburgh.
AfME are advertising for a Research Director.
https://www.actionforme.org.uk/get-information/about-us/work-or-volunteer-with-us/
Research Director
Hours of work: Full-time, 35hrs a week
Location: Home-based or Keynsham office
Salary: £50,000
Be honest, have you ever heard about M.E.? Many...
I'm impressed by the Coronavirus APPG website (https://www.appgcoronavirus.uk/). It looks like Best For Britain are providing the secretariat, and the fancy website, which is interesting.
The ME Association and AfME have just confirmed that they are continuing to provide the secretariat for the...
I know Keith has struggled for funding. It is not easy in academia, and it's probably worse in field a like ME/CFS. But I have no idea what he's applied for, how his proposals were rated, and why they were rejected. I also don't know if he's applied for salaried positions such as fellowships. I...
I've not followed this, but there are further shenanigans involving IncellDx / Patterson, regarding some sort of blood draw clinic in the UK for long-covid and/or vaccine-injured people. It looks like each party is blaming each other.
Unfortunately my step-Dad passed away recently. I'm now helping my mum with lots of things including finances etc.
I believe she is entitled to part of my step-Dad's state pension. They married before 2016 (which seems to be a cut-off), and my step-Dad reached state pension age before April...
I agree. I think BACME could be a worthwhile organisation *if they get it right*. BACME is the only form of central orgsanisation within the NHS system for ME/CFS patients as all the clinics and specialist services are individual entities commissioned by local CCGs and run by individual trusts...
Next BACME event: Journal Club: Hartle, M.; Bateman, L. and Vernon, S.D. (2021) Dissecting the nature of post-exertional malaise.
https://www.bacme.info/civicrm/event/info?id=20
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